Department of Chemistry, University of Cambridge , Lensfield Road, Cambridge, U.K. CB2 1EW.
J Am Chem Soc. 2016 Feb 17;138(6):1955-61. doi: 10.1021/jacs.5b12423. Epub 2016 Feb 3.
Sodium batteries have seen a resurgence of interest from researchers in recent years, owing to numerous favorable properties including cost and abundance. Here we examine the feasibility of studying this battery chemistry with in situ NMR, focusing on Na metal anodes. Quantification of the NMR signal indicates that Na metal deposits with a morphology associated with an extremely high surface area, the deposits continually accumulating, even in the case of galvanostatic cycling. Two regimes for the electrochemical cycling of Na metal are apparent that have implications for the use of Na anodes: at low currents, the Na deposits are partially removed on reversing the current, while at high currents, there is essentially no removal of the deposits in the initial stages. At longer times, high currents show a significantly greater accumulation of deposits during cycling, again indicating a much lower efficiency of removal of these structures when the current is reversed.
近年来,由于成本和丰富度等诸多优势,钠离子电池重新引起了研究人员的兴趣。在这里,我们研究了使用原位 NMR 研究这种电池化学的可行性,重点是研究 Na 金属阳极。NMR 信号的定量分析表明,Na 金属沉积物具有与极高表面积相关的形态,即使在恒流循环的情况下,沉积物也会不断积累。Na 金属电化学循环的两种状态明显存在,这对 Na 阳极的使用有影响:在低电流下,反转电流时部分去除 Na 沉积物,而在高电流下,初始阶段基本上不会去除沉积物。在较长时间内,高电流显示出在循环过程中沉积物的显著积累,这再次表明当电流反转时,这些结构的去除效率明显降低。